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临床试验/NCT03764865
NCT03764865已完成不适用

Day 3 vs Day 5 Embryo Transfer for Patients With Low Embryo Numbers Going Through in Vitro Fertilization (PILOT STUDY)

Beth Israel Deaconess Medical Center1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2021年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
1
主要终点
live birth

研究概览

简要总结

The purpose of this small-scale pilot study (10 patients) is to test the study protocol for an RCT comparing IVF outcomes between day 3 and day 5 embryo transfer in patients with five or fewer embryos in a fresh embryo transfer in vitro fertilization (IVF) cycle. Information derived from this RCT would allow us to maximize the chances of success for these patients undergoing IVF.

详细描述

Embryos created with assisted reproductive technology (ART, e.g. in vitro fertilization (IVF)) are commonly transferred into a woman's uterus at either the cleavage stage (day 3 after egg retrieval) or blastocyst stage (day 5 after egg retrieval). Until recently, most IVF cycles transferred embryos at the cleavage stage. However, with improvements in in vitro culture technique there has been a steady shift in practice to transfer embryos at the blastocyst stage (day 5 after egg retrieval) as this timing is about the same as when embryos reach the endometrial cavity in natural conception.

There now is a general consensus that, for good prognosis patients, those with a high embryo from the IVF cycle, it is beneficial to transfer the embryo on day 5 rather than day 3. The rationale for this is to allow for self-selection of embryos, meaning those that develop to blastocyst in vitro are more likely to be viable in vivo and result in a viable pregnancy. In addition, transferring an embryo on day 5 improves uterine/embryonic synchronicity and thereby improves outcomes. This allows the transfer of fewer embryos and decreases the likelihood of multiples (twins, triplets, etc.).

As a result, day 5 transfer has become standard of care for good prognosis patients in the United States. The American Society of Reproductive Medicine1 issued a committee opinion in 2013 to this effect stating that in "good prognosis" patients, blastocyst transfer results in a significant increase in live birth rates compared to transfer of an equal number of cleavage stage embryos (50.5% vs. 30.1%, P< .01)2-5. In addition, for unselected and poor prognosis patients, no high-quality studies have evaluated whether blastocyst transfer increases live birth rates when compared to cleavage stage transfer.

It is possible that the attrition of day 3 embryos in vivo is lower than the attrition in vitro and that day 5 transfer leads to loss of embryos that may have survived in vivo. In addition, women undergoing blastocyst culture are expected to have a higher incidence of cycle cancellation due to failure of the embryo to develop to a blastocyst6 and of having fewer embryos cryopreserved (frozen)7. Because of this, in Europe and Asia, day 3 transfer is the most common practice.

On the other hand, transferring embryos on day 3 decreases our ability to select the best embryo, increases laboratory costs and may increase multiple pregnancy rates as, typically, more embryos are transferred at this time. In addition, in vivo, day 3 embryos are in transit through the fallopian tube during natural conception and are exposed to a different developmental and nutritional environment than day 3 IVF embryos transferred into the uterine cavity. Thus, it is possible that exposing day 3 embryos to the physiologically premature uterine environment (particularly one that has been subjected to superovulation and thus high levels of estrogen) increases embryo attrition compared to day 5 transfer, particularly in poor prognosis patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 44 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •First autologous IVF cycle
  • •Written, informed consent

排除标准

  • •Planned gestational carrier
  • •Planned donor egg
  • •Morbid obesity: BMI >40
  • •History of recurrent pregnancy loss (≥2 spontaneous abortions)
  • •Presence of uterine factor infertility
  • •Treatment plan includes embryos cultured 'out of protocol'
  • •Planned preimplantation genetic testing

研究组 & 干预措施

day 3 embryo transfer

Experimental

embryo transfer 3 days after fertilization

干预措施: day 3 uterine transfer (Procedure)

day 5 embryo transfer

Experimental

embryo transfer 5 days after fertilization

干预措施: day 5 uterine transfer (Procedure)

结局指标

主要结局

live birth

时间窗: 9 months

defined as delivery of a live born infant ≥22 weeks of gestation

次要结局

  • Clinical pregnancy(14 days)
  • Time to pregnancy/live birth(2 years)
  • Ongoing pregnancy(9 months)
  • Multiple pregnancy(9 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Werner Neuhausser

Instructor in Obstetrics, Gynecology and Reproductive Biology

Beth Israel Deaconess Medical Center

研究点 (1)

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